Proposed Information Collection Activity; Comment Request, 24976-24977 [2017-11234]

Download as PDF 24976 Federal Register / Vol. 82, No. 103 / Wednesday, May 31, 2017 / Notices leading causes of death for the first four decades of life, regardless of gender, race, or socioeconomic status. More than 192,000 individuals in the United States die each year as a result of unintentional injuries and violence, and more than 31 million others suffer nonfatal injuries requiring emergency department visits each year. This collection is to collect information needed for programmatic activities of the Regional Network Coordinating Organization (RNCO) enhanced component funded under the well as qualitative summaries. Information to be collected will provide crucial data for program planning and continuous quality improvement of program. The data will also provide CDC with the capacity to respond in a timely manner to requests for information about the program from the Department of Health and Human Services (HHS), the White House, Congress, and other sources. The only cost to respondents will be time spent responding to the survey. Core State Violence and Injury Prevention Program (Core SVIPP) cooperative agreement (CDC–RFA– CE16–1602) Member entities (state health departments at their partners) of the RNCO awardees will respond to a membership survey annually. Member entities of the RNCO awardees will also participate in annual focus groups to inform and contribute to National Peer Learning Teams (NPLT). No research design or human subjects are involved. The data will be analyzed using descriptive and summary statistics as ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Average burden per response (hours) Number of responses per respondent Total burden (hours) Type of respondents Instrument name RNCO Member Survey ..................... RNCO NLPT Focus Group Protocol Annual RNCO and NPLT Survey ..... Annual NPLT Member Focus Group Protocol. 250 125 1 1 3 1.5 750 188 Total ........................................... ........................................................... ........................ ........................ ........................ 938 Leroy A. Richardson, Chief, Information Collection Review Office, Office of Scientific Integrity, Office of the Associate Director for Science,Office of the Director, Centers for Disease Control and Prevention. [FR Doc. 2017–11110 Filed 5–30–17; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Proposed Information Collection Activity; Comment Request Proposed Projects: Title: Child and Family Services Plan (CFSP), Annual Progress and Services Review (APSR), and Annual Budget Expenses Request and Estimated Expenditures (CFS–101). OMB No.: 0970–0426. Description: Under title IV–B, subparts 1 and 2, of the Social Security Act (the Act), States, Territories, and Tribes are required to submit a Child and Family Services Plan (CFSP). The CFSP lays the groundwork for a system of coordinated, integrated, and culturally relevant family services for the subsequent five years (45 CFR 1357.15(a)(1)). The CFSP outlines initiatives and activities the State, Tribe or territory will carry out in administering programs and services to promote the safety, permanency, and well-being of children and families, including, as applicable, those activities conducted under the John H. Chafee Foster Care Independence Program (Section 477 of the Act) and the State grant authorized by the Child Abuse Prevention and Treatment Act. By June 30 of each year, States, Territories, and Tribes are also required to submit an Annual Progress and Services Report (APSR) and a financial report called the CFS–101. The APSR is a yearly report that discusses progress made by a State, Territory or Tribe in accomplishing the goals and objectives cited in its CFSP (45 CFR 1357.16(a)). The APSR contains new and updated information about service needs and organizational capacities throughout the five-year plan period. The CFS–101 has three parts. Part I is an annual budget request for the upcoming fiscal year. Part II includes a summary of planned expenditures by program area for the upcoming fiscal year, the estimated number of individuals or families to be served, and the geographical service area. Part III includes actual expenditures by program area, numbers of families and individuals served by program area, and the geographic areas served for the last complete fiscal year. Respondents: States, Territories, and Tribes must complete the CFSP, APSR, and CFS–101. Tribes and territories are exempted from the monthly caseworker visits reporting requirement of the CFSP/APSR. There are approximately 189 Tribal entities that currently receive IV–B funding. There are 53 States (including Puerto Rico, the District of Columbia, and the Virgin Islands) that must complete the CFSP, APSR, and CFS–101. There are a total of 242 possible respondents. ANNUAL BURDEN ESTIMATES Number of respondents nlaroche on DSK30NT082PROD with NOTICES Instrument APSR ............................................................................................................... CFSP ............................................................................................................... CFS–101, Parts I, II, and III ............................................................................ Caseworker Visits ............................................................................................ VerDate Sep<11>2014 14:54 May 30, 2017 Jkt 241001 PO 00000 Frm 00043 Fmt 4703 Sfmt 4703 Number of responses per respondent 242 242 242 53 E:\FR\FM\31MYN1.SGM 1 1 1 1 31MYN1 Average burden hours per response 80 120.25 5 99.33 Total burden hours 19,360 29,100.50 1,210 5,264.49 Federal Register / Vol. 82, No. 103 / Wednesday, May 31, 2017 / Notices Estimated Total Annual Burden Hours: 54,934.99. In compliance with the requirements of Section 506(c)(2)(A) of the Paperwork Reduction Act of 1995, the Administration for Children and Families is soliciting public comment on the specific aspects of the information collection described above. Copies of the proposed collection of information can be obtained and comments may be forwarded by writing to the Administration for Children and Families, Office of Planning, Research and Evaluation, 330 C Street SW., Washington, DC 20202; Attn: ACF Reports Clearance Officer. Email address: infocollection@acf.hhs.gov. All requests should be identified by the title of the information collection. The Department specifically requests comments on: (a) Whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information shall have practical utility; (b) the accuracy of the agency’s estimate of the burden of the proposed collection of information; (c) the quality, utility, and clarity of the information to be collected; and (d) ways to minimize the burden information to be collected; and (d) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information technology. Consideration will be given to comments and suggestions submitted within 60 days of this publication. Robert Sargis, Reports Clearance Officer. [FR Doc. 2017–11234 Filed 5–30–17; 8:45 am] BILLING CODE 4184–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2010–N–0623] Agency Information Collection Activities; Proposed Collection; Comment Request; Voluntary Cosmetic Registration Program AGENCY: Food and Drug Administration, nlaroche on DSK30NT082PROD with NOTICES HHS. ACTION: Notice. The Food and Drug Administration (FDA or Agency) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of SUMMARY: VerDate Sep<11>2014 14:54 May 30, 2017 Jkt 241001 1995 (PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice invites comments on the collection of information associated with our Voluntary Cosmetic Registration Program (VCRP). DATES: Submit either electronic or written comments on the collection of information by July 31, 2017. ADDRESSES: You may submit comments as follows. Please note that late, untimely filed comments will not be considered. Electronic comments must be submitted on or before July 31, 2017. The https://www.regulations.gov electronic filing system will accept comments until midnight Eastern Time at the end of July 31, 2017. Comments received by mail/hand delivery/courier (for written/paper submissions) will be considered timely if they are postmarked or the delivery service acceptance receipt is on or before that date. Electronic Submissions Submit electronic comments in the following way: • Federal eRulemaking Portal: https://www.regulations.gov/. Follow the instructions for submitting comments. Comments submitted electronically, including attachments, to https://www.regulations.gov/ will be posted to the docket unchanged. Because your comment will be made public, you are solely responsible for ensuring that your comment does not include any confidential information that you or a third party may not wish to be posted, such as medical information, your or anyone else’s Social Security number, or confidential business information, such as a manufacturing process. Please note that if you include your name, contact information, or other information that identifies you in the body of your comments, that information will be posted on https://www.regulations.gov/. • If you want to submit a comment with confidential information that you do not wish to be made available to the public, submit the comment as a written/paper submission and in the manner detailed (see ‘‘Written/Paper Submissions’’ and ‘‘Instructions’’). Written/Paper Submissions Submit written/paper submissions as follows: • Mail/Hand delivery/Courier (for written/paper submissions): Division of PO 00000 Frm 00044 Fmt 4703 Sfmt 4703 24977 Dockets Management (HFA–305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. • For written/paper comments submitted to the Division of Dockets Management, FDA will post your comment, as well as any attachments, except for information submitted, marked and identified, as confidential, if submitted as detailed in ‘‘Instructions.’’ Instructions: All submissions received must include the Docket No. FDA– 2010–N–0623 for ‘‘Agency Information Collection Activities; Proposed Collection; Comment Request; Voluntary Cosmetic Registration Program.’’ Received comments, those filed in a timely manner (see ADDRESSES), will be placed in the docket and, except for those submitted as ‘‘Confidential Submissions,’’ publicly viewable at https:// www.regulations.gov/ or at the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday. • Confidential Submissions—To submit a comment with confidential information that you do not wish to be made publicly available, submit your comments only as a written/paper submission. You should submit two copies total. One copy will include the information you claim to be confidential with a heading or cover note that states ‘‘THIS DOCUMENT CONTAINS CONFIDENTIAL INFORMATION.’’ The Agency will review this copy, including the claimed confidential information, in its consideration of comments. The second copy, which will have the claimed confidential information redacted/blacked out, will be available for public viewing and posted on https://www.regulations.gov/. Submit both copies to the Division of Dockets Management. If you do not wish your name and contact information to be made publicly available, you can provide this information on the cover sheet and not in the body of your comments and you must identify this information as ‘‘confidential.’’ Any information marked as ‘‘confidential’’ will not be disclosed except in accordance with 21 CFR 10.20 and other applicable disclosure law. For more information about FDA’s posting of comments to public dockets, see 80 FR 56469, September 18, 2015, or access the information at: https://www.gpo.gov/ fdsys/pkg/FR-2015-09-18/pdf/201523389.pdf. Docket: For access to the docket to read background documents or the electronic and written/paper comments received, go to https:// www.regulations.gov/ and insert the docket number, found in brackets in the E:\FR\FM\31MYN1.SGM 31MYN1

Agencies

[Federal Register Volume 82, Number 103 (Wednesday, May 31, 2017)]
[Notices]
[Pages 24976-24977]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-11234]

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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families

Proposed Information Collection Activity; Comment Request

Proposed Projects:
Title: Child and Family Services Plan (CFSP), Annual Progress and
Services Review (APSR), and Annual Budget Expenses Request and
Estimated Expenditures (CFS-101).
OMB No.: 0970-0426.
Description: Under title IV-B, subparts 1 and 2, of the Social
Security Act (the Act), States, Territories, and Tribes are required to
submit a Child and Family Services Plan (CFSP). The CFSP lays the
groundwork for a system of coordinated, integrated, and culturally
relevant family services for the subsequent five years (45 CFR
1357.15(a)(1)). The CFSP outlines initiatives and activities the State,
Tribe or territory will carry out in administering programs and
services to promote the safety, permanency, and well-being of children
and families, including, as applicable, those activities conducted
under the John H. Chafee Foster Care Independence Program (Section 477
of the Act) and the State grant authorized by the Child Abuse
Prevention and Treatment Act. By June 30 of each year, States,
Territories, and Tribes are also required to submit an Annual Progress
and Services Report (APSR) and a financial report called the CFS-101.
The APSR is a yearly report that discusses progress made by a State,
Territory or Tribe in accomplishing the goals and objectives cited in
its CFSP (45 CFR 1357.16(a)). The APSR contains new and updated
information about service needs and organizational capacities
throughout the five-year plan period. The CFS-101 has three parts. Part
I is an annual budget request for the upcoming fiscal year. Part II
includes a summary of planned expenditures by program area for the
upcoming fiscal year, the estimated number of individuals or families
to be served, and the geographical service area. Part III includes
actual expenditures by program area, numbers of families and
individuals served by program area, and the geographic areas served for
the last complete fiscal year.
Respondents: States, Territories, and Tribes must complete the
CFSP, APSR, and CFS-101. Tribes and territories are exempted from the
monthly caseworker visits reporting requirement of the CFSP/APSR. There
are approximately 189 Tribal entities that currently receive IV-B
funding. There are 53 States (including Puerto Rico, the District of
Columbia, and the Virgin Islands) that must complete the CFSP, APSR,
and CFS-101. There are a total of 242 possible respondents.

Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average
Instrument Number of responses per burden hours Total burden
respondents respondent per response hours
----------------------------------------------------------------------------------------------------------------
APSR............................................ 242 1 80 19,360
CFSP............................................ 242 1 120.25 29,100.50
CFS-101, Parts I, II, and III................... 242 1 5 1,210
Caseworker Visits............................... 53 1 99.33 5,264.49
----------------------------------------------------------------------------------------------------------------

[[Page 24977]]

Estimated Total Annual Burden Hours: 54,934.99.
In compliance with the requirements of Section 506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Administration for Children and
Families is soliciting public comment on the specific aspects of the
information collection described above. Copies of the proposed
collection of information can be obtained and comments may be forwarded
by writing to the Administration for Children and Families, Office of
Planning, Research and Evaluation, 330 C Street SW., Washington, DC
20202; Attn: ACF Reports Clearance Officer. Email address:
infocollection@acf.hhs.gov. All requests should be identified by the
title of the information collection.
The Department specifically requests comments on: (a) Whether the
proposed collection of information is necessary for the proper
performance of the functions of the agency, including whether the
information shall have practical utility; (b) the accuracy of the
agency's estimate of the burden of the proposed collection of
information; (c) the quality, utility, and clarity of the information
to be collected; and (d) ways to minimize the burden information to be
collected; and (d) ways to minimize the burden of the collection of
information on respondents, including through the use of automated
collection techniques or other forms of information technology.
Consideration will be given to comments and suggestions submitted
within 60 days of this publication.

Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2017-11234 Filed 5-30-17; 8:45 am]
BILLING CODE 4184-01-P

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